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Autor:
Mohamed M. Abd Elrahman, Aida I. El makawy, Mohamed S. Hassanane, Sally S. Alam, Nagwa H. A. Hassan, Medhat K. Amer
Publikováno v:
Journal of Genetic Engineering and Biotechnology, Vol 19, Iss 1, Pp 1-15 (2021)
Abstract Background Asthenozoospermia is a chief reason for male seminal pathologies with an impression of around 19% of infertile patients. Spermatozoa mitochondrial DNA variations seem to link with low sperm motility. The objective of the study was
Externí odkaz:
https://doaj.org/article/86424f7abc44455c873b9e22051b9c90